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Cited 102 time in webofscience Cited 113 time in scopus
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Direct Imaging of Cerebral Thromboemboli Using Computed Tomography and Fibrin-targeted Gold Nanoparticlesopen access

Authors
Kim, Jeong-YeonRyu, Ju HeeSchellingerhout, DawidSun, In-CheolLee, Su-KyoungJeon, SangminKim, JiwonKwon, Ick ChanNahrendorf, MatthiasAhn, Cheol-HeeKim, KwangmeyungKim, Dong-Eog
Issue Date
2015
Publisher
IVYSPRING INT PUBL
Keywords
direct thrombus imaging; gold nanoparticles; computed tomography; cerebral infarction; molecular imaging
Citation
THERANOSTICS, v.5, no.10, pp 1098 - 1114
Pages
17
Indexed
SCIE
SCOPUS
Journal Title
THERANOSTICS
Volume
5
Number
10
Start Page
1098
End Page
1114
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/19225
DOI
10.7150/thno.11679
ISSN
1838-7640
Abstract
Computed tomography (CT) is the current standard for time-critical decision-making in stroke patients, informing decisions on thrombolytic therapy with tissue plasminogen activator (tPA), which has a narrow therapeutic index. We aimed to develop a CT-based method to directly visualize cerebrovascular thrombi and guide thrombolytic therapy. Glycol-chitosan-coated gold nanoparticles (GC-AuNPs) were synthesized and conjugated to fibrin-targeting peptides, forming fib-GC-AuNP. This targeted imaging agent and non-targeted control agent were characterized in vitro and in vivo in C57BI/6 mice (n = 107) with FeCl3-induced carotid thrombosis and/or embolic ischemic stroke. Fibrin-binding capacity was superior with fib-GC-AuNPs compared to GC-AuNPs, with thrombi visualized as high density on microCT (mCT). mCT imaging using fib-GC-AuNP allowed the prompt detection and quantification of cerebral thrombi, and monitoring of tPA-mediated thrombolytic effect, which reflected histological stroke outcome. Furthermore, recurrent thrombosis could be diagnosed by mCT without further nanoparticle administration for up to 3 weeks. fib-GC-AuNP-based direct cerebral thrombus imaging greatly enhance the value and information obtainable by regular CT, has multiple uses in basic/translational vascular research, and will likely allow personalized thrombolytic therapy in clinic by a) optimizing tPA-dosing to match thrombus burden, b) enabling the rational triage of patients to more radical therapies such as endovascular clot-retrieval, and c) potentially serving as a theranostic platform for targeted delivery of concurrent thrombolysis.
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